"Ambry Genetics"[submitter] AND "MS4A15"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2361066	NM_001098835.2(MS4A15):c.7G>C (p.Ala3Pro)	MS4A15 (A3P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2551319	NM_001098835.2(MS4A15):c.26G>A (p.Gly9Glu)	MS4A15 (G9E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2349707	NM_001098835.2(MS4A15):c.55G>A (p.Ala19Thr)	MS4A15 (A19T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3210562	NM_001098835.2(MS4A15):c.56C>A (p.Ala19Asp)	MS4A15 (A19D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2533937	NM_001098835.2(MS4A15):c.91A>G (p.Thr31Ala)	MS4A15 (T31A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2213489	NM_001098835.2(MS4A15):c.109C>T (p.Pro37Ser)	MS4A15 (P37S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2476714	NM_001098835.2(MS4A15):c.158G>A (p.Arg53Lys)	MS4A15 (R53K)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2602460	NM_001098835.2(MS4A15):c.182G>T (p.Arg61Leu)	MS4A15 (R61L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2406769	NM_001098835.2(MS4A15):c.206G>A (p.Gly69Glu)	MS4A15 (G69E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2311412	NM_001098835.2(MS4A15):c.227C>T (p.Thr76Met)	MS4A15 (T76M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212019	NM_001098835.2(MS4A15):c.290G>A (p.Arg97His)	MS4A15 (R97H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2456074	NM_001098835.2(MS4A15):c.329C>A (p.Pro110His)	MS4A15 (P110H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3210534	NM_001098835.2(MS4A15):c.365C>T (p.Ser122Phe)	MS4A15 (S81F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612215	NM_001098835.2(MS4A15):c.377C>T (p.Ala126Val)	MS4A15 (A126V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210541	NM_001098835.2(MS4A15):c.436A>G (p.Ser146Gly)	MS4A15 (S53G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519999	NM_001098835.2(MS4A15):c.443T>G (p.Met148Arg)	MS4A15 (M107R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406054	NM_001098835.2(MS4A15):c.449C>T (p.Ala150Val)	MS4A15 (A150V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341043	NM_001098835.2(MS4A15):c.484G>A (p.Gly162Ser)	MS4A15 (G69S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2315119	NM_001098835.2(MS4A15):c.512G>C (p.Gly171Ala)	MS4A15 (G130A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3210570	NM_001098835.2(MS4A15):c.680C>T (p.Pro227Leu)	MS4A15 (P227L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601369	NM_001098835.2(MS4A15):c.686C>T (p.Ala229Val)	MS4A15 (A136V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2272321	NM_001098835.2(MS4A15):c.700G>A (p.Ala234Thr)	MS4A15 (A234T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598036	NM_001098835.2(MS4A15):c.715G>A (p.Val239Ile)	MS4A15 (V198I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 23